Pathophysiological Mechanisms of Antipsychotic-Induced Parkinsonism
1V. M. Bekhterev National Medical Research Center for Psychiatry and Neurology, Institute of Personalized Psychiatry and Neurology, 192019 St. Petersburg, Russia
2Shared Core Facilities Molecular and Cell Technologies, V.F. Voyno-Yasenetsky Krasnoyarsk State Medical University, 660022 Krasnoyarsk, Russia
3International Centre for Education and Research in Neuropsychiatry, Samara State Medical University, 443079 Samara, Russia
4Department of Physiotherapy, Faculty of Continuing Medical Education, Peoples’ Friendship University of Russia, 117198 Moscow, Russia
5Department of Medical Genetics and Clinical Neurophysiology, Institute of Postgraduate Education, V.F. Voyno-Yasenetsky Krasnoyarsk State Medical University, 660022 Krasnoyarsk, Russia
6Department of Neurology and Neurosurgery, Siberian State Medical University, 634050 Tomsk, Russia
*Correspondence: vaimanelenadoc@gmail.com (E.E.V.); naschnaider@yandex.ru (N.A.S.); nreginaf77@gmail.com (R.F.N.); Tel.: +7-(812)-620-02-20-78-13 (E.E.V., N.A.S. & R.F.N.)Abstract
Among neurological adverse reactions in patients with schizophrenia treated with antipsychotics (APs), drug-induced parkinsonism (DIP) is the most common motility disorder caused by drugs affecting dopamine receptors. One of the causes of DIP is the disruption of neurotransmitter interactions that regulate the signaling pathways of the dopaminergic, cholinergic, GABAergic, adenosinergic, endocannabinoid, and other neurotransmitter systems. Presently, the development mechanisms remain poorly understood despite the presence of the considered theories of DIP pathogenesis.
1. Introduction
Drug-induced parkinsonism (DIP), tardive dyskinesia (TD), tardive dystonia, akathisia, myoclonus, and tremor are drug-induced motility disorders. Among these adverse drug reactions (ADR), DIP is the most widespread movement disorder caused by drugs that antagonise dopamine receptors, after Parkinson’s disease (PD), which has similar clinical manifestations [1,2]. That is why patients with DIP are often misdiagnosed as having PD [1,3]. These patients often took antiparkinsonian drugs for a long period of time, despite the fact that recovery is possible simply by stopping the offending medicinal drugs. Antipsychotics (APs) are the most common cause of DIP. Antipsychotic-induced parkinsonism (AIP) usually manifests itself within a few days or weeks after the start of AP, but in rare cases, the delay in onset can be several months or more [4]. Moreover, the complexity of differential diagnosis arises between DIP and negative symptoms of schizophrenia or withdrawal syndrome, as well as with depression [5].
AIP debuts in patients older than 40 years, women are two times more committed than men [6]. Despite the development of APs of new generations, the problem of AIP has not been solved to date. As shown in Table 1, all APs have a potential risk of AIP ranging from low (+) to high (+++).
Due to the fact that APs of the first and new generations affect different mechanisms of action in the treatment of schizophrenia spectrum disorders, the risk of developing AIP in some APs of new generations remains high, almost similar to APs of the first generation. This may be due to the fact that the pathophysiological mechanisms of AIP development are more complex than previously thought. In addition to the effect of AP on dopaminergic neurons, other possible mechanisms are being considered (Figure 1). Knowledge of these mechanisms can help in the development of new personalized strategies for the prediction, prevention and early correction of AIP in patients with schizophrenia spectrum, which will improve the therapeutic response and quality of life of the patient. This was the reason for the preparation of this thematic review, the purpose of which is to analyze basic and clinical studies studying on the pathophysiological mechanisms of AIP.
One of the causes of AIP is a disruption of neurotransmitter interactions that regulate the signaling pathways of the dopaminergic, cholinergic, GABA-ergic, adenosinergic, endocannabinoid and other neurotransmitter systems. The monoamine (dopamine, serotonin, and norepinephrine) systems of the brain play an important role in normal behavior, and disturbances in these circuits are thought to be involved in the development of a number of neurological and psychiatric disorders. The dopamine system is involved in the implementation of such brain functions as locomotion, affect and cognition. It is also known that this system is the last monoamine system that is formed in the brain during ontogeny [7], which suggests that it can have an important stabilizing and integrative effect on brain circuits, and that its disruption can cause their dysfunction [8]. Dopamine neurons in the substantia nigra in its dorsal part are associated with the limbic and cortical or associative systems of the brain, while those in the ventral part are associated with motility [9].
1.1. Dopamine D2 Type Receptors Blockade
Dopamine receptors in the brain are represented by two families: the D1 (D1 family receptors and D5 receptors), and the D2 (D2, D3 and D4 receptors). All currently available APs are able to antagonize dopamine D2 receptors, and the APs’ therapeutic effects in psychosis are related to their action on the limbic system reducing dopamine transmission. Due to antagonism of dopamine D2 receptors in the striatum, neurons of gamma aminobutyric acid (GABA), encephalin and the subthalamic nucleus are disinhibited at the beginning of the indirect pathway without changing the direct pathway. Due to this, there is an increase in GABA inhibition in the thalamocortical projection by facilitating inhibition in the globus pallidus/reticular substantia nigra. This pathway is similar to the model of basal ganglia motor loop impairment in PD [4].
It is assumed that the mechanism of action of APs is associated with the level of occupancy of the dopamine D2 receptors. This is confirmed by several reports that therapeutic doses of typical APs block D2 receptors in 70–89% of cases in young adults, while atypical APs block in 38–63% of cases [10].
1.2. Supersaturation (“Occupancies”) of Striatal Dopamine D2/3 Receptors
The exact mechanism of AIP development is still unknown; nevertheless, the main theory is the dopamine receptors blockade. In animal models, about 70% of the occupancy of dopamine D2/3 receptors was recorded during AP therapy, which leads to the development of AIP [11]. The threshold levels of occupancy of dopamine D2/3 receptors in the striatum associated with the development of AIP in young adults, which is about 80%, have been demonstrated in studies using neuroimaging technologies (using positron emission tomography (PET) D2/3 receptor imaging) [12,13]. Dissimilarities in the severity of AIP development are associated with the occupancy density of dopamine D2/3 receptors, AP concentration, the rate of dissociation from the D2 receptor, the selectivity of dopamine receptors in the limbic system and striatum, and the activity of other receptors (for example, serotonergic, muscarinic) [14]. Therefore, typical APs are more associated with an increased risk of developing AIP than atypical APs [14,15,16]. However, such a high occupancy of dopamine receptors should not be considered unequivocally, because the occupancy of receptors is not equal to antagonism. For example, aripiprazole, which, in addition to dopamine receptors, interacts with serotonin (5-HT) types 1A and 2A receptors and rarely causes AIP, even with a dopamine receptor occupancy rate > 95% due to a weak antagonistic effect on dopamine receptors [17,18].
1.3. Influence of the Basal Ganglia of the Thalamocortical Motor Loop
The pathophysiology of AIP is associated with drug-induced changes in the motor chain of the basal ganglia secondary to blockade of dopaminergic receptors [4]. The central dopaminergic system is presented of the four pathways: mesolimbic, mesocortical, tuberoinfundibular, and nigrostriatal (Figure 2).
When dopamine D2 receptors blockade in the striatum, striatal neurons containing GABA and encephalin are disinhibited, affecting the indirect pathway and ultimately leading to a relative decrease in the activity of thalamocortical circuits [4,19]. This effect may be mitigated by APs anticholinergic activity [20,21], as evidenced by the observation that clozapine has a low risk of developing AIP and also has a high relative affinity for muscarinic cholinergic receptors [20]. The reason for the decrease in sufficient concentrations of dopamine in the striatum may also be a decrease in the release of dopamine into the synaptic cleft [21]. Drugs that do not directly affect dopamine levels (valproic acid, calcium channel blockers) can induce DIP through other mechanisms, including modulation of GABA activity or mitochondrial dysfunction (Figure 3) [4,21,22,23,24].
1.4. Fast-off-D Theory
In studies devoted to brain occupancy, radioactive clozapine has been proven to show rapid and transient occupancy of the dopamine D2 type receptors, dissociating in less than 60 s after administration, while radioactive haloperidol and chlorpromazine show long-term occupancy with slow dissociation in less than 30 min. Therefore, atypical APs are clinically more effective, having temporary occupancy of D2 type dopamine receptors and rapid dissociation to normal dopamine neurotransmission (Table 2) [26,27].
1.5. Role of Adenosine Receptors
Purine and adenosine interact with major neurotransmitter systems (glutamatergic cholinergic, GABA-ergic and dopaminergic) to modulate neuronal function in the central and peripheral nervous systems [28].
Transmission of adenosine occurs through purinergic receptors coupled to the G-protein class P1, which is subdivided into four receptor subtypes: A1, A2A, A2B, and A3 [29]. A2A adenosine receptors are highly expressed by GABAergic neurons in the striatum, globus pallidus, and olfactory bulb [30], and are co-localized with dopamine D2 type receptors in the basal ganglia on enkephalin-expressing output neurons of the indirect pathway leading to the globus pallidus and substantia nigra [31,32], which are in dopaminergic nigrostriatal and mesolimbic neuronal pathways [33]. The A2A and D2 receptors are antagonists and regulate GABA neurons [34,35].
Most evidence suggests that due to intramembrane interaction, activation of the adenosine A2A receptor indirectly blocks the activation of dopamine D2 receptors, and stimulation of D2 receptors blocks the activation of adenylate cyclase caused by the A2A receptor [34]. Upon stimulation of A2A receptors, GABA is released, while upon stimulation of D2 receptors, it is suppressed in the globus pallidus [35,36]. Here is evidence that these receptors, on the contrary, can act as synergists, under certain circumstances (presence of certain isoforms of adenylate cyclase, interruption of previous long-term exposure to D2 receptor agonists), activation of the D2 receptors enhances the effects of A2A receptors [34]. A study by Parsons et al. [37] in rats showed that chronic administration of haloperidol activates striatal A2A receptors. The effect of haloperidol was selective for A2A receptors over other adenosine receptor subtypes. Notably, atypical APs did not affect A2A receptors’ density in this study [37]. A2A adenosine receptor antagonists suppress motor disorders such as catalepsy and locomotion induced by dopamine antagonists [38,39]. A2A receptor antagonists are effective in relieving muscle rigidity and tremor in AIP (Figure 4) [15,40,41].
1.6. Blockade of the Serotonergic System
The serotonergic system plays a crucial role in various physiological actions regulation, including psychoemotional, cognitive, sensorimotor, and autonomic functions [42,43,44]. Serotonergic neurotransmission is presented by several 5-HT receptors, which are classified into 7 families (5-HT1 to 5-HT7) and 14 subtypes (5-HT1A, 1B, 1D, 1E, 1F, 5-HT2A, 2B, 2C, 5-HT4, 5-HT3, 5-HT5A, 5B, 5-HT6 and 5-HT7) [45,46]. The 5-HT1E, 5-HT1F, and 5-HT5 receptors are associated with the Gi/o protein and inhibit adenylate cyclase activity, cyclic adenosine monophosphate (cAMP) formation, and protein kinase A (PKA) activity. The 5-HT2A, 5-HT2B, and 5-HT2C receptors are coupled to the Gq protein and increase phosphatidylinositol (PI) turnover by activating phospholipase C, thereby stimulating the protein kinase C− and Ca2+/calmodulin cascade. The 5-HT4, 5-HT6, and 5-HT7 receptors are Gs-coupled and activate adenylate cyclase and PKA [44,45,46].
5-HT1A receptors are localized in the raphe nucleus, hippocampus, amygdala, and lateral septum. Expression of 5-HT1A receptors occurs in the cerebral cortex, basal ganglia (striatum), and diencephalon (thalamus and hypothalamus) in low to moderate density [42,47,48]. Inhibition of adenylate cyclase activity by 5-HT1A receptors leads to inhibition of the cAMP-PKA cascade. In addition, 5-HT1A receptors activate G-protein-gated inwardly rectifying potassium channels (GIRK), which hyperpolarize target neurons and suppress their activity [41,43,44,45]. Several studies on animal models have shown that 5-HT1A receptors are activated with the introduction of AP for dehydration, has a protective effect on the development of extrapyramidal syndrome (EPS) [49,50,51,52,53,54,55]. The 5-HT2A and 5-HT2C receptors are highly expressed in the cerebral cortex, olfactory tubercle and limbic system (nucleus accumbens, hippocampus), basal ganglia (striatum and substantia nigra). 5-HT2A/2C antagonists attenuate AP-induced EPS in PD patients [56,57,58] by increasing the level of released acetylcholine, dopamine metabolism, and Fos protein expression in the striatum [57]. 5-HT3 receptors constitute a heteropentamer consisting of subunits from 5-HT3A to 5-HT3E and function as a cation (Na+, K+, and Ca2+) permeable channels [45,59]. Therefore, when 5-HT3 receptors are activated, postsynaptic membranes are depolarized, thereby exciting target neurons. Serotonin 5-HT3 receptors are located in the nerve endings of various neurons and induce the release of neurotransmitters (acetylcholine, glutamate, GABA and dopamine). Clinical studies have also shown that 5-HT3 receptor antagonists significantly reduce the frequency and severity of AP-induced EPS (e.g., AIP) in patients with chronic schizophrenia [60,61]. However, a recent study showed that serotonin 5-HT3 receptors do not affect the activity of cholinergic interneurons in the striatum [62]. Thus, the functional mechanisms of 5-HT3 receptors in EPS are still unclear. The expression of serotonin 5-HT6 receptors mainly occurs in the brain, in particular, in the basal ganglia (striatum and nucleus accumbens), limbic system (olfactory tubercles and hippocampus), and cerebral cortex [45]. According to the results of clinical studies, 5-HT6 receptor antagonists also have a protective property against the development of EPS [63,64]. The decrease in the incidence and severity of EPS in the presence of 5-HT6 antagonists was further confirmed by an electrophysiological study [62], reflecting a decrease in the activation of striatal acetylcholine neurons, thereby reducing the likelihood of developing EPS (Figure 5) [65].
Agonists of postsynaptic and presynaptic serotonin 5-HT1A receptors lead to a de-crease in the manifestations of extrapyramidal movement disorders. This is explained by hyperpolarization GABA medial spine neurons or indirectly by inhibition acetylcholinergic and glutamatergic interneurons in the striatum. In addition, when presynaptic 5-HT1A autoreceptors are stimulated, the serotonergic activity of neurons in the nuclei of the sutures is inhibited, reducing the functions of 5-HT2A/2C, 5-HT3 and 5-HT6 receptors, as a result of which the symptoms of extrapyramidal movement disorders improve.
1.7. Cholinergic Theory
The desired blockade of the mesolimbic pathways leads to simultaneous inhibition of dopamine D2 type receptors in the substantia nigra, resulting in AIP. Cholinergic interneurons in the basal ganglia balance dopaminergic activity. Accordingly, in PD, when the balance is disturbed due to the degeneration of dopaminergic neurons, there is a relative predominance of cholinergic activity. Thus, the pathogenesis in PD can be considered as both a lack of dopaminergic activity and a relative increase in cholinergic activity.
Based on this theory, cholinergic drugs can also be prescribed to patients in order to restore the balance of the dopaminergic and cholinergic systems [66].
1.8. Melatonin Theory
Melatonin interacts with 5-HT2 receptors and can regulate the activity of dopamine. In case of higher concentrations, melatonin acts as a 5-HT2 receptor antagonist and leads to an increase in dopaminergic activity, while at physiological concentrations, melatonin reduces dopamine, acting as an agonist. These modulating effects of melatonin on dopamine activity may explain the circadian changes in dopamine activity [67,68] and the circadian changes in the clinical course in patients with schizophrenia treated with APs; as a result, a reduction in the symptom severity can be expected [69]. Animal studies indicate that APs interfere with melatonin secretion. In rats, APs sharply increase melatonin levels in the pineal gland and blood plasma [70]. Similarly, in humans, plasma melatonin levels increase during AP therapy [71]. As a result of antagonism of the 5-HT2 receptor by high concentrations of melatonin, dopamine activity will increase, thereby counteracting the blockade of dopamine receptors caused by APs. Thus, the interaction between the decrease in dopamine activity during the use of APs, and the protective effect of therapeutic concentrations of melatonin on dopamine function in the form of its increase, may partially explain the delay in AP effects, the delayed appearance of AIP, and possibly the regression of AIP. However, because chronic use of APs (for more than 6 months) can eventually damage the cells of the pineal gland [72], it can be expected that melatonin secretion will decrease, which will contribute to ADRs in the background of AP. In confirmation of this theory, clinical examples are presented, where patients with AIP risk factors associated with reduced melatonin secretion (older age, postmenopausal women, depression [73]) had a history of AIP more often [74,75,76,77].
1.9. Theory of Oxidative Stress
The theory of oxidative stress is actively studied in the pathogenesis of extrapyramidal movement disorders. Despite the fact that damage to cellular structures is observed during oxidative stress, its components act as second messengers in the formation of regulatory functions. One of the free radicals of oxidative stress that regulates various cellular signaling pathways is nitric oxide (NO) [78]. When NO synthase is inhibited, enzyme activity is reduced by 80%, leading to the formation of primary and secondary products of lipid peroxidation (conjugated dienes (CD) and trienes (CT), malondialdehyde (MDA) and Schiff bases (SB)). According to the study by Dolgo-Saburov et al. [79], a significant increase in the concentration of CD and CT is observed after blockade of the dopamine D2 type receptors while taking APs in the studied structures of the central nervous system. The accumulation of MDA and SB also indicates the development of oxidative stress and its maintenance after a decrease in NO synthase activity [79]. Haloperidol-induced AIP is associated with elevated levels of the haloperidol metabolite, pyridinium, which is toxic to dopamine neurons [80,81]. This toxic metabolite can be produced locally in the brain [82]. During haloperidol therapy, oxidative metabolism in the brain increases [83], protein kinase B (Akt) phosphorylation decreases, which leads to caspase-3 activation [84]. Haloperidol alters the expression of the transcription nuclear factor kappa B (NF-κB) in the substantia nigra, which directly affects oxidative stress [85] and plays a role in the activation of several genes involved in the immune and inflammatory systems [86].
1.10. Role of Vitamin D3
The vitamin D3 receptor (VDR) is a widespread steroid receptor, mainly localized in the pigmented nigrostriatal tract and motor cortex [87,88], providing melanin synthesis, cytoskeletal stability, and calcium in the motor area [89]. Indirectly, the control of calcium during the inhibition of NMDA receptors (NMDAR) in the elimination of excitotoxicity in vitro and in vivo has been described [90,91]. In addition, NMDAR enhancement is involved in glutamate excitotoxicity, degeneration in the nigrostriatal tract and motor cortex by increasing inward calcium flow, thereby increasing the level of calcium in the brain [92]. Activation of VDR by its agonists and inhibition of NMDAR in vitro reduces calcium toxicity and stabilizes microtubules, with a protective effect against excitotoxicity and synaptic denervation [93,94,95]. Reducing the reversibility of cortical degeneration (parkinsonism) with calcium supplementation mediated by VDR and NMDAR is still relatively unexplored [96]. Potentiation of VDR and inhibition of NMDAR reduce the level of toxicity in the cerebral cortex by improving neuronal metabolism, the amount of glia and the cytoskeleton to support synaptic function, thus increasing neural activity and motor-cognitive functions. Against the background of taking AP, synaptic denervation occurs due to a calcium-dependent depolymerization of microtubules in motor neurons [97]. It also increases the activity of glia and cells, leading to inflammation [98,99]. Motor ADR in the presence of APs may be the result of antagonism of D2 type dopamine receptors, resulting in the induction of oxidative stress and increased production of free radicals (ROS) [100] due to which the concentration of calcium ions increases both intracellularly and extracellularly [101,102]. This accumulation of calcium leads to microtubule collapse and excessive phosphorylation of the microtubule-associated protein tau, which is involved in the stabilization of the structure of axons and dendrites [103,104]. Recent studies have established an interaction between elevated calcium levels, autophagy, and synaptic denervation in the pathogenesis of AIP [90,91,105]. Elevated calcium and glutamate concentrations, combined with low serum vitamin D3 levels, are associated with the risk of developing parkinsonism and other neurodegenerative diseases [106,107,108].
1.11. Genetic Theory
The role of genetic risk factors in the mechanisms of development of AIP [109] has been known for more than 40 years. This was also confirmed by later studies [110,111,112]. Individual differences in susceptibility to haloperidol-induced parkinsonism were explained by individual pharmacokinetic variability associated with the influence of carriage of single nucleotide variants (SNVs) of the CYP3A4 and CYP3A5 genes, which affects the metabolism of haloperidol to its pyridinium ion. While taking haloperidol, pyridinium ion-related toxicity may be observed, which may be exacerbated in patients on polytherapy with antidepressants, as they interact with this system [6,86,113,114,115,116].
Moreover, at the moment, other associations of candidate genes for the risk of developing AIP have already been studied, shown in Figure 6.
In our systematic review, the following positive associations for the risk of developing AIP were noted: rs1799732 (NG_008841.1:g.4750dup), rs1800497 (NG_012976.1:g.17316G>A), rs6275 (NG_008841.1:g.67525T>C) of the DRD2 gene; rs167771 (NG_008842.2:g.46980C>T, NG_008842.2:g.46980C>G, NG_008842.2:g.46980C>A) of the DRD3 gene; rs4680 (NG_011526.1:g.27009G>A) of the COMT gene; rs6311 (NG_013011.1:g.4692G>T, NG_013011.1:g.4692G>A) of the 5HTR2A gene; rs6318 (NG_012082.2:g.152242G>C, NG_012082.2:g.152242G>T) and rs3813929 (NG_012082.2:g.4963C>G, NG_012082.2:g.4963C>T) of the HTR2C gene; rs2179652 (NG_022822.1:g.225C>T), rs2746073 (NG_012800.1:g.6059T>A), rs4606 (NG_012800.1:g.8004C>G, NG_012800.1:g.8004C>T), rs1152746 (NC_000001.11:g.192827775C>G, NC_000001.11:g.192827775C>T), rs1819741 (NC_000001.11:g.192815708T>A, NC_000001.11:g.192815708T>A) and rs1933695 (NC_000001.11:g.192795690G>A) of the RGS2 gene; rs4795390 (NG_030330.1:g.3434G>A, NG_030330.1:g.3434G>C, NG_030330.1:g.3434G>T) of the PPP1R1B gene; rs6265 (NG_011794.1:g.68690G>A) of the BDNF gene; rs12678719 (NG_011723.2:g.189908C>G) of the ZFPM2 gene; rs938112 (NC_000003.12:g.117129003C>A, NC_000003.12:g.117129003C>T) of the LSMAP gene; rs2987902 (NG_012034.1:g.125979A>T) of the ABL1 gene. However, at present, it should be recognized that there is no definitive or single decision on the leading role of any particular SNVs/polymorphisms in AIP development [6,114,116,117].
2. Discussion
In terms of motor function disorders, AIP and AP-induced TD are the most common neurological ADRs associated with APs use. However, to the present date, it remains unclear which patient and against the background of taking which specific AP one or another ADRs will develop. The pathophysiological mechanisms of AIP and AP-induced TD are different. While there is a decrease in the function of the extrapyramidal system in the form of the development of bradykinesia, muscle rigidity in AIP, in AP-induced TD, on the contrary, there is an increase in function in the form of violent movements [118]. It has been shown that long-term use of AP is associated with the formation of ROS as a result of increased metabolism of catecholamines (Figure 7). The reduction in such oxidative damage to AP-sensitive dopaminergic neurons has become the basis of antioxidant treatment for AP-induced TD. However, the effectiveness of AIP antioxidant therapy is low. While AIP results from the interaction of APs with substantia nigra neurons, dyskinetic symptoms may also be more closely related to AP-induced problems in the striatum, in particular the caudate nucleus [23,66].
It should be assumed that the development of AIP in patients with schizophrenia is influenced by such risk factors as taking APs of the first generation (in 50% of patients AIP eventually develops while taking APs); elderly age; genetic predisposition; a history of human immunodeficiency virus infection. On the other hand, when predicting the development of AIP, one should take into account not only the risk factors, but also protective factors of AIP: taking anticholinergic drugs (due to increased cholinergic activity, which leads to stimulation of the GABA-ergic inhibitory pathway in the basal ganglia); smoking (nicotine can act as an inhibitor of monoamine oxidase B, increasing the availability of dopamine) [28]. In recent decades, genetic predictors of AIP and AP-induced TD have been actively studied as a risk for the development of these neurological ADRs [120,121,122].
The theories of AIP development discussed in this review are very important. First of all, knowledge about the AIP pathogenesis can help with better understanding of the disease nature. Moreover, thanks to the understanding of the pathogenetic mechanisms of AIP, new opportunities for the treatment of this ADR are opening up. At the same time, knowledge about the pathogenesis of AIP can help to develop personalized strategies for the correction of patients suffering from AIP or at risk of developing AIP. Despite the large number of theories presented, the pathogenetic mechanism of this neurological ADR remains unclear.
Thus, it is impossible to single out one of the theories as the dominant mechanism for the development of AIP. Undoubtedly, the pathophysiology of AIP should be considered as an interconnected complex of neurotransmitter systems (dopamine, serotonin, adenosine, acetylcholine, and others) that affect each other and depend on nonmodifiable risk factors—gender, age, genetic predisposition—as well as modifiable ones—the type of AP, its dose, concomitant diseases, etc. At the same time, knowledge of this raises questions about the personalized risks of developing AIP in a particular patient because the pathophysiological mechanisms of developing AIP may differ in different patients. Thus, this poses new challenges and requires additional research to better understand the molecular pathophysiology of AIP.
The limitations for this review were the difficulties in finding full-text publications and the presence of abstracts that did not reveal the full information of the theories of pathogenesis. Moreover, in many similar works, information is duplicated in a compressed version. For a complete understanding of the pathogenetic mechanisms, it would be interesting to consider the differences, taking into account the gender and age of patients with AIP. We did not find any articles with reliable data assessing differences by sex and age in this review, which are the predictors of the risk of developing AIP. Thus, a review of these theories is relevant, but we have not found such works.
In this review, we have described the pathogenetic mechanisms of AIP development found in the literature and presented the theories in as much detail as possible with the help of figures and tables for better understanding.
3. Conclusions
Our review of studies of the mechanisms of AIP development in an animal model and patients with schizophrenia allows us to identify the following theories: impaired function of D2 type dopamine receptors (blockade of D2 type dopamine receptors, supersaturation of D2 type dopamine receptors, “Fast-off-D2” theory); dysfunction of the basal ganglia of the thalamocortical motor loop; dysfunction of adenosine receptors; blockade of serotonergic receptors; cholinergic theory; oxidative stress; violation of melatonin metabolism; violation of the level of vitamin D3; genetic theory. The search for the leading pathophysiological mechanisms of AIP is important for the development of a personalized strategy, prevention, therapy, considered neurological ADRs of AP-therapy in real clinical practice.
Institutional Review Board Statement
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Informed Consent Statement
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Data Availability Statement
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Conflicts of Interest
The authors declare no conflict of interest.
| Antipsychotics of First Generation | Risk of Developing AIP | Antipsychotics of New Generations | Risk of Developing AIP |
|---|---|---|---|
| Haloperidol | +++ | Lurasidone | ++ |
| Pimozide | +++ | Olanzapine | ++ |
| Thiothixene | +++ | Paliperidone | ++ |
| Fluphenazine | +++ | Risperidone | ++ |
| Loxapin | ++ | Azenapine | + |
| Molindon | ++ | Aripiprazole | + |
| Perphenazine | ++ | Brexpiprazole | + |
| Trifluoperazine | ++ | Ziprasidone | + |
| Chlorpromazine | ++ | Iloperidone | + |
| Thioridazine | + | Karipazin | + |
| Quetiapine | + | ||
| Clozapine | + | ||
| Lumateperone | + | ||
| Pimavenzirin | + |
| Antipsychotics | Occupancy Percentage (%) | ||
|---|---|---|---|
| D2 Receptors | D3 Receptors | D4 Receptors | |
| Clozapine | 38–63 | 62 | 49–73 |
| Chlorpromazine | 78 | 62 | 17 |
| Haloperidol | 85 | 52 | 57 |
| Olanzapine | 43–89 | 10–55 | 27–80 |
| Risperidone | 63–89 | 25–61 | 22–55 |
| Quetiapine | 51 | 24 | 88 |